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Development of a qPCR assay to detect and quantify Paenibacillus riograndensis DH44, and the effect of drought on Peanut soil fungal diversity.


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dc.contributor.advisorNoel, Zachary
dc.contributor.authorDabargainya, Bibek
dc.date.accessioned2025-12-02T19:42:16Z
dc.date.available2025-12-02T19:42:16Z
dc.date.issued2025-12-02
dc.identifier.urihttps://etd.auburn.edu/handle/10415/10069
dc.description.abstractPlant health is not only determined by the plant itself, but also by its interaction with the surrounding microbial environment. These communities comprise various microbes, including bacteria and fungi, that inhabit different niches, such as the rhizosphere, endosphere, and phyllosphere. They help regulate various functions, including nutrient cycling, hormone balance, and stress tolerance, yet they are influenced by environmental drivers such as water availability, temperature, and soil chemistry. Drought, in particular, thins water films, alters diffusion and exudation, and reassembles microbial networks, with consequences for crop performance and disease risk. Harnessing and studying beneficial microbes, therefore, requires not only an ecological understanding of when and where communities shift, but also the use of tools and techniques to detect, quantify, and track key taxa in complex plant-soil matrices. Chapter 1 provides a review of previous literature, including peanut biology and drought physiology, as well as plant growth-promoting rhizobacteria, with an emphasis on Paenibacillus. It also discusses how moisture influences plant-associated microbiomes. Chapter 2 focuses on designing and developing a qPCR tool for detecting the Paenibacillus reograndensis DH44 strain. This strain has been researched for its potential as a biofertilizer in bermudagrass. Using K-mer Exclusion by Cross-referencing (KEC) comparative genomics, we screened 1122 Paenibacillus genomes, identifying unique regions in DH44 and designing two primer pairs: KEC12 and KEC13, with primer efficiencies of 99.4% and 90.08%, respectively. The assay limit of detection was 124 cell copies per reaction and was successfully validated in planta, with qPCR signals closely correlating with CFU plate count estimates. In chapter 3, we were able to distinguish the fungal communities in peanut habitats (pegs, roots, and adjacent soil) under mid-season drought versus irrigated treatment over three years (2022-2024), sampling both a drought-tolerant and a drought sensitive variety at the Auburn University Plant Breeding Unit, Tallassee, AL. Water status and habitat were the major differentiating factors, whereas variety effects were minimal as a main effect and appeared primarily as an interaction with another factor. Mid-season drought resulted in a modest change in overall diversity, but a clear variation in community composition, with the pegs showing the most consistent separation over the years. Furthermore, the differential abundance of peg tissue showed a shift toward stress-tolerant, endophytic lineages under drought (e.g., Alternaria, Acremonium, Tilachlidium), while irrigation favored moisture-responsive and opportunistic taxon profiles (Colletotrichum, Nothopassalora), underscoring water availability as the dominant ecological filter of the peanut microbiome. Finally, Chapter 4 discusses the overall conclusions and impacts.en_US
dc.rightsEMBARGO_NOT_AUBURNen_US
dc.subjectEntomology and Plant Pathologyen_US
dc.titleDevelopment of a qPCR assay to detect and quantify Paenibacillus riograndensis DH44, and the effect of drought on Peanut soil fungal diversity.en_US
dc.typeMaster's Thesisen_US
dc.embargo.lengthMONTHS_WITHHELD:24en_US
dc.embargo.statusEMBARGOEDen_US
dc.embargo.enddate2027-12-02en_US
dc.contributor.committeeDe La Fuente, Leonardo
dc.contributor.committeeDillard, Leanne

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